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NM_032119.4:c.11599G>A
MANE Select
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NP_115495.3:p.Glu3867Lys
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ENST00000405460.9:c.11599G>A
MANE Select
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ENSP00000384582.2:p.Glu3867Lys
|
|
NM_032119.3:c.11599G>A
|
NP_115495.3:p.Glu3867Lys
|
|
NR_003149.1:n.11612G>A
|
|
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NR_003149.2:n.11615G>A
|
|
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ENST00000405460.6:c.11599G>A
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ENSP00000384582.2:p.Glu3867Lys
|
|
ENST00000425867.3:c.712-507G>A
|
ENSP00000392618.3:n.712-507G>A
|
|
ENST00000509621.1:c.4296G>A
|
|
|
ENST00000639431.1:c.265+80263G>A
|
ENSP00000491057.1:n.265+80263G>A
|
|
ENST00000640374.1:n.4725-507G>A
|
|
|
ENST00000640464.1:n.2018G>A
|
|
|
XM_011543675.1:c.11596G>A
|
XP_011541977.1:p.Glu3866Lys
|
|
XM_011543676.1:c.11518G>A
|
XP_011541978.1:p.Glu3840Lys
|
|
XM_011543677.1:c.8902G>A
|
XP_011541979.1:p.Glu2968Lys
|
|
XM_011543678.1:c.11599G>A
|
XP_011541980.1:p.Glu3867Lys
|
|
XM_017009963.2:c.11620G>A
|
XP_016865452.1:p.Glu3874Lys
|
|
XM_017009964.2:c.11617G>A
|
XP_016865453.1:p.Glu3873Lys
|
|
XM_017009965.1:c.11617G>A
|
XP_016865454.1:p.Glu3873Lys
|
|
XM_017009966.2:c.11539G>A
|
XP_016865455.1:p.Glu3847Lys
|
|
XM_017009967.1:c.11524G>A
|
XP_016865456.1:p.Glu3842Lys
|
|
XM_017009968.2:c.11620G>A
|
XP_016865457.1:p.Glu3874Lys
|
|
XM_017009969.2:c.11620G>A
|
XP_016865458.1:p.Glu3874Lys
|
|
XM_017009970.2:c.11620G>A
|
XP_016865459.1:p.Glu3874Lys
|
|
XM_017009971.2:c.11620G>A
|
XP_016865460.1:p.Glu3874Lys
|
|
XM_017009972.1:c.4738G>A
|
XP_016865461.1:p.Glu1580Lys
|
|
XM_017009973.1:c.4717G>A
|
XP_016865462.1:p.Glu1573Lys
|